Anomalies of the long arm of chromosome 11 in human myelo- and lymphoproliferative disorders. I: Acute nonlymphocytic leukemia = Anomalies du bras long du chromosome 11 dans les affections myélo- et lymphoprolifératives. I. Leucémie aiguë non lymphoïdeVERMAELEN, K; BARBIERI, D; MICHAUX, J.-L et al.Cancer genetics and cytogenetics. 1983, Vol 10, Num 1, pp 105-116, issn 0165-4608Article

The 11q; 22q translocation: a collaborative study of 20 new cases and analysis of 110 familiesISELIUS, L; LINDSTEN, J; DUTRILLAUX, B et al.Human genetics. 1983, Vol 64, Num 4, pp 343-355, issn 0340-6717Article

Partial deletion of the long arm of chromosome 11: prenatal diagnosisCHUDLEY, A. E; PABELLO, P. D; PINNO, E et al.American journal of medical genetics. 1983, Vol 16, Num 1, pp 137-139, issn 0148-7299Article

TOPOGRAPHIC VARIATIONS IN THE CLONOGENIC RESPONSE OF INTESTINAL CRYPTS TO CYTOTOXIC TREATMENTS = VARIATIONS TOPOGRAPHIQUES DE LA REPONSE CLONOGENIQUE DES CRYPTES INTESTINALES AUX TRAITEMENTS CYTOTOXIQUESMOORE JV; MAUNDA KKY.1983; BRITISH JOURNAL OF RADIOLOGY; ISSN 0007-1285; GBR; DA. 1983; VOL. 56; NO 663; PP. 193-199; ABS. ENG; BIBL. 15 REF.; GRAPHArticle

IN VITRO INHIBITION OF MISONIDAZOLE TOXICITY AND MELPHALAN CHEMOPOTENTATION BY METYRAPONE = INHIBITION, IN VITRO, DE LA TOXICITE DU MISONIDAZOLE ET CHIMIOPOTENTIALISATION DU MELPHALAN PAR LA METYRAPONEMILLAR BC; JINKS S.1983; BRITISH JOURNAL OF RADIOLOGY; ISSN 0007-1285; GBR; DA. 1983; VOL. 56; NO 663; PP. 201-206; ABS. ENG; BIBL. 20 REF.; GRAPHArticle

DEUX NOUVEAUX CAS DE MONOSOMIE 11Q PARTIELLE AVEC POINT DE CASSURE EN 11Q24LAURENT C; BIEMONT MC; VEYRON M et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 4; PP. 239-241; ABS. ENG; BIBL. 13 REF.Article

DEPLETION OF CELLULAR THIOLS BY MISONIDAZOLE TREATMENT PREVENTS SOME POST-IRRADIATION REPAIR PROCESSES = LA DEPLETION EN THIOLS CELLULAIRES PAR TRAITEMENT PAR MISONIDAZOLE EMPECHE QUELQUES PROCESSUS DE REPARATION POST-IRRADIATIONEDGREN M.1983; BRITISH JOURNAL OF RADIOLOGY; ISSN 0007-1285; GBR; DA. 1983; VOL. 56; NO 663; PP. 211-212; BIBL. 10 REF.; GRAPHArticle

Chromosomes in myelodysplastic syndrome: structural abnormalities of chromosome 11MUSILOVA, J; MICHALOVA, K; JAROSOVA, M et al.Annales de génétique (Paris). 1989, Vol 32, Num 1, pp 43-46, issn 0003-3995, 4 p.Article

Translocation t(11;14) and trisomy 11q13→qter in multiple myelomaVENTI, G; MECUCCI, C; DONTI, E et al.Annales de génétique (Paris). 1984, Vol 27, Num 1, pp 53-55, issn 0003-3995Article

Interstitial deletion of 11qGUC-SCEKIC, M; PILIC-RADIVOJEVIC, G; MRDJENOVIC, G et al.Journal of medical genetics. 1989, Vol 26, Num 3, pp 205-206, issn 0022-2593, 2 p.Article

Deficiency of all or part of chromosome 11 in several types of cancer: significance of a reduction in the number of normal chromosomes 11ATKIN, N. B; BAKER, M. C.Cytogenetics and cell genetics. 1988, Vol 47, Num 1-2, pp 106-107, issn 0301-0171Article

ISOLATED PERIPHERAL THROMBOCYTOPENIA AS PRESENTING SYMPTOM IN PRELEUKEMIA: A REPORT OF TWO CASES WITH 11Q+TRICOT G; VAN DEN BERGHE H.1982; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1982; VOL. 5; NO 2; PP. 147-151; BIBL. 8 REF.Article

PARTIAL MONOSOMY OF THE LONG ARM OF CHROMOSOME 11 IN A SEVERELY AFFECTED CHILDLEE ML; SCIORRA LJ.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 1; PP. 51-53; ABS. FRE; BIBL. 4 REF.Article

DUPLICATION U(0,21 TO 23->QTER) SYNDROME.FRANCKE U; WEBER F; SPARKES RS et al.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3B; PP. 167-186; BIBL. 12 REF.Article

FAMILIAL PERICENTRIC INVERSION OF CHROMOSOME 11 DETECTED PRENATALLYRUSSEL MH; MILLER R; KILLAM A et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 2; PP. 151-152; BIBL. 8 REF.Article

ABSENCE OF CONSTITUTIVE HETEROCHROMATIN IN A PARTIALLY IDENTIFIED SUPERNUMERARY MARKER CHROMOSOMEPAL GS; THOMAS GH; BENKE P et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 5; PP. 392-394; BIBL. 7 REF.Article

DELETION OF THE LONG ARM OF CHROMOSOME 11: A CLINICAL ENTITYFELDING I; MITELMAN F.1979; ACTA PAEDIATR. SCAND.; SWE; DA. 1979; VOL. 68; NO 4; PP. 635-638; BIBL. 11 REF.Article

RING 11 CHROMOSOME (46,XX,R11(P15Q25).VALENTE M; MULLER H; SPARKES RS et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 3; PP. 345-350; BIBL. 12 REF.Article

TWO PERICENTRIC INVERSIONS OF HUMAN CHROMOSOME 11.SIMOLA K; KARLI P; DE LA CHAPELLE A et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 5; PP. 371-374; BIBL. 15 REF.Article

CONGENITAL GLAUCOMA AND OTHER OCULAR ABNORMALITIES ASSOCIATED WITH PERICENTRIC INVERSION OF CHROMOSOME 11BROUGHTON WL; ROSENBAUM KN; BEAUCHAMP GR et al.1983; ARCHIVES OF OPHTHALMOLOGY; ISSN 0003-9950; USA; DA. 1983; VOL. 101; NO 4; PP. 594-597; BIBL. 33 REF.Article

ASSOCIATION NEPHROBLASTOME-ANIRIDIE CHEZ DES MALADES PORTEURS DE DELITION DU CHROMOSOME 11ZHORDANIA RV; KULAGINA OE; BUKHNY AE et al.1981; GENETIKA; ISSN 0016-6758; SUN; DA. 1981; VOL. 17; NO 7; PP. 1315-1317; ABS. ENG; BIBL. 8 REF.Article

A NEW CHROMOSOME ABNORMALITY IN IDIOPATHIC SIDEROBLASTIC ANEMIA: 46, XY, DEL 11Q23HYDER DM; BOTTOMLEY SS; BOTTOMLEY RH et al.1978; AMER. J. HEMATOL.; USA; DA. 1978; VOL. 5; NO 3; PP. 239-245; BIBL. 22 REF.Article

PERICENTRIC INVERSION OF CHROMOSOME 11 IN ONE OF TWO SIMILAR RETARDED BROTHERSEINFELD SL; SMITH A.1982; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 4; PP. 312; BIBL. 3 REF.Article

BALANCED AND UNBALANCED PERICENTRIC INVERSION OF CHROMOSOME 11FRYNS JP; HASPESLAGH M; GODDEERIS P et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 3; PP. 182-183; ABS. FRE; BIBL. 6 REF.Article

A POSSIBLE SPECIFIC CHROMOSOME MARKER FOR MONOCYTIC LEUKEMIA: THREE MORE PATIENTS WITH T(9;11) (P22;Q24) AND ANOTHER WITH T(11;17) (Q24;Q21), EACH WITH ACUTE MONOBLASTIC LEUKEMIA = UN POSSIBLE MARQUEUR CHROMOSOMIQUE SPECIFIQUE DE LA LEUCEMIE MONOCYTAIRE: TROIS MALADES EN PLUS AVEC T(9;11) (P22;Q24) ET UN AUTRE AVEC T(11;17) (Q24;Q21), TOUS ETANT ATTEINTS DE LEUCEMIE AIGUE MONOBLASTIQUEDEWALD GW; MORRISON DELAP SJ; SCHUCHARD KA et al.1983; CANCER GENETICS AND CYTOGENETICS; ISSN 0165-4608; NLD; DA. 1983; VOL. 8; NO 3; PP. 203-212; ABS. ENG; BIBL. 7 REF.; FIGArticle